cancer: causes and treatment. causes of mutations: replication errors –exacerbated by poor dna...
TRANSCRIPT
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Cancer: causes and treatment
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Causes of mutations:
• Replication errors– Exacerbated by poor DNA repair
• Other biological agents– Viruses– Transposons
• Environmental factors– Ultraviolet light– Mutagenic chemicals
• smoking, industrial waste, natural toxins
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Change in the US Death Rates* by Cause, 1950 & 2000
* Age-adjusted to the 2000 US standard population.Source: US Mortality Volume 1950, National Vital Statistics Report, 2002, Vol. 50, No. 15.
586.8
180.5
48.160.923.7
200.9193.7
258.2
0
100
200
300
400
500
600
HeartDiseases
Stroke Pneumonia/Influenza
Cancer
1950
2000
Rate Per 100,000
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Cancer Death Rates*, for Men, US, 1930-1999
*Age-adjusted to the 2000 US standard population.Source: US Mortality Public Use Data Tapes 1960-1999, US Mortality Volumes 1930-1959, National Center for Health Statistics, Centers for Disease Control and Prevention, 2002.
0
20
40
60
80
100
1930 1935 1940 1945 1950 1955 1960 1965 1970 1975 1980 1985 1990 1995
Lung
Colon and rectum
Prostate
Pancreas
Stomach
Liver
Rate Per 100,000
Leukemia
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Cancer Death Rates*, for Women, US, 1930-1999
*Age-adjusted to the 2000 US standard population.Source: US Mortality Public Use Data Tapes 1960-1999, US Mortality Volumes 1930-1959, National Center for Health Statistics, Centers for Disease Control and Prevention, 2002.
0
20
40
60
80
100
1930 1935 1940 1945 1950 1955 1960 1965 1970 1975 1980 1985 1990 1995
Lung
Colon and rectum
Uterus
Stomach
Breast
Ovary
Pancreas
Rate Per 100,000
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Tobacco Use in the US, 1900-1999
0
500
1000
1500
2000
2500
3000
3500
4000
4500
5000
190019051910191519201925193019351940194519501955196019651970197519801985199019952000Year
Per Capita Cigarette Consumption
0
10
20
30
40
50
60
70
80
90
100
Age-Adjusted Lung Cancer Death
Rates*
*Age-adjusted to 2000 US standard population.
Source: Death rates: US Mortality Public Use Tapes, 1960-1999, US Mortality Volumes, 1930-1959, National Center for Health Statistics, Centers for Disease Control and Prevention, 2001. Cigarette consumption: Us Department of Agriculture, 1900-1999.
Per capita cigarette consumption
Male lung cancer death rate
Female lung cancer death rate
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Tobacco Use in the US, 1900-1999
0
500
1000
1500
2000
2500
3000
3500
4000
4500
5000
190019051910191519201925193019351940194519501955196019651970197519801985199019952000Year
Per Capita Cigarette Consumption
0
10
20
30
40
50
60
70
80
90
100
Age-Adjusted Lung Cancer Death
Rates*
*Age-adjusted to 2000 US standard population.
Source: Death rates: US Mortality Public Use Tapes, 1960-1999, US Mortality Volumes, 1930-1959, National Center for Health Statistics, Centers for Disease Control and Prevention, 2001. Cigarette consumption: Us Department of Agriculture, 1900-1999.
Per capita cigarette consumption
Male lung cancer death rate
Female lung cancer death rate
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Treating cancer:• Avoid it
– Avoid mutagens– DNA repair gets less efficient as we age
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T-cells recognize and eliminate abnormal cells; such as cells with many mutations
Our immune system protects us from cancer
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Treating cancer:• Avoid it
– Avoid mutagens– DNA repair gets less efficient as we age
• Surgery– Must remove all cancer cells– Non-invasive
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Treating cancer:• Avoid it
– Avoid mutagens– DNA repair gets less efficient as we age
• Surgery– Must remove all cancer cells– Non-invasive
• Radiation– Directed at tumor; causes DNA damage
-> cellular self-destruction– Mutagenic, side effects
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Treating cancer:• Avoid it
– Avoid mutagens– DNA repair gets less efficient as we age
• Surgery– Must remove all cancer cells– Non-invasive
• Radiation– Directed at tumor – Mutagenic, side effects
• Chemotherapy– Toxins directed at rapidly dividing cells– Mutagenic, many side effects
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Chemotherapy
a rapidly dividing cell
Toxin
X X
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Normal Multi-Drug Resistance protein
MDR
MD
RMDR
MD
R
toxin/hormone/etc
toxin/hormone/etc
toxin/h
ormon
e/etc
toxin/h
ormon
e/etc
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Some cancers over-express MDR
Toxin
MDR
MD
R
MDRMDRMDR
MD
RMDRMDRMDRMDR
MD
RM
DR
toxin toxin
toxin toxin toxin toxin
toxin
toxin
toxin
toxin
toxin toxin
I’m a cancer cell with over-expressing MDR. I laugh at your toxins.
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The Epigenetic Progenitor Origin of Human Cancer (2007) A P Feinberg, R Ohlsson, S Henikoff Nature Reviews Genetics 7: 21-31
Mutations continue after cancer develops
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O
O
OOO
O
O
OO
OOCancer cell with mutation causing MDR over-production
Evolution: changes in DNA as information transmitted
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O
O
OOO
O
O
OO
OO
O
O
OOO
O
O
OO
OO
Applychemotherapy
XXX
XX X XX
XX
Kills most cells. Except if some have mutation that allow them to be resistant.
Evolution: changes in DNA as information transmitted
Cancer cell with mutation causing MDR over-production
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O
O
OOO
O
O
OO
OO
O
O
OOO
O
O
OO
OO
O
XXX
XX X XX
XX
Kills most cells. Except if some have mutation that allow them to be resistant.
Continues to replicate
Evolution: changes in DNA as information transmitted
Applychemotherapy
Cancer cell with mutation causing MDR over-production
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O
O
OOO
O
O
OO
OO
O
O
OOO
O
O
OO
OO
O
O
OOO
O
O
OO
OO
O
XXX
XX X XX
XX
Kills most cells.
Continues to replicate
Tumor with cells expressing MDR
Evolution: changes in DNA as information transmitted
Applychemotherapy
Cancer cell with mutation causing MDR over-production
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Some cancers over-express MDR
Toxin
MDR
MD
R
MDRMDRMDR
MD
RMDRMDRMDRMDR
MD
RM
DR
toxin toxin
toxin toxin toxin toxin
toxin
toxin
toxin
toxin
toxin toxin
I’m a cancer cell with over-expressing MDR. I laugh at your toxins.
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Treating cancer:• Avoid it
– Avoid mutagens– DNA repair gets less efficient as we age
• Surgery– Must remove all cancer cells– Non-invasive
• Radiation– Directed at tumor – Mutagenic, side effects
• Chemotherapy– Toxins directed at rapidly dividing cells– Mutagenic, many side effects
![Page 26: Cancer: causes and treatment. Causes of mutations: Replication errors –Exacerbated by poor DNA repair Other biological agents –Viruses –Transposons Environmental](https://reader036.vdocuments.us/reader036/viewer/2022081519/56649efc5503460f94c0f3c6/html5/thumbnails/26.jpg)
Multiple mutations are required for a single cell to become cancerous.
CB18.22
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How can mutations be minimized?
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Telomeres are non-gene DNA at the ends of DNA strands.
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Telomeres are non-gene DNA at the ends of DNA strands.
Telomeres are shortened during DNA replication.
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Telomeres are non-gene DNA at the ends of DNA strands.
Telomeres are shortened during DNA replication, and also by DNA damage.
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Telomeres are non-gene DNA at the ends of DNA strands.
Short telomeres will cause cells to stop replicating or cell death.
The critical size is unknown.
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HumanLifeCycle
high levels of telomerase
very little telomerase
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Why not produce telomerase all of the time?
high levels of telomerase
very little telomerase
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Telomeres are non-gene DNA at the ends of DNA strands.
Telomeres are shortened during DNA replication, and by DNA damage.
Short telomeres will cause cell senescence or cell death.Telomere size is an indirect measure of mutations.
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Fig. 3 TRENDS in Ecology and Evolution Vol 21 pg 47
Balance between Longevity and Health
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Do telomere dynamics link lifestyleand lifespan?
Pat Monaghan and Mark F. HaussmannTRENDS in Ecology and Evolution
Vol 21 pg 47
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Telomere length varies in different parts of adults:
telomeres - mitosisstomach &blood cells....short - often
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Telomere length varies in different parts of adults:
telomeres - mitosisstomach &blood cells....short - often
muscle &brain……….long - rare
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Telomere length varies in different parts of adults:
telomeres - mitosisstomach &blood cells....short - often
muscle &brain……….long - rare
liver &kidney……..short - rare
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Telomere length varies in different parts of adults:
telomeres - mitosisstomach &blood cells....short - often
muscle &brain……….long - rare
liver &kidney……..short - rare
gametes……long
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Zebra finch
Telomere length in red blood cells of different birds
Fig. 1 TRENDS in Ecology and Evolution Vol 21 pg 47
Age (years)
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common tern
Telomere length in red blood cells of different birds
Fig. 1 TRENDS in Ecology and Evolution Vol 21 pg 47
Age (years)
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albatross
TRENDS in Ecology and Evolution Vol 21 pg 47
Telomere length in red blood cells of different birds
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Leach’s storm petrel
Telomere length in red blood cells of different birds
Fig. 1 TRENDS in Ecology and Evolution Vol 21 pg 47
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Zebra finch
Leach’s storm petrel
common tern
albatross
Telomere length in red blood cells of different birds, different species have different patterns of telomere length and age
Fig. 1 TRENDS in Ecology and Evolution Vol 21 pg 47
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Fig. 2 TRENDS in Ecology and Evolution Vol 21 pg 47
Telomere length in white blood cells of different aged people. Telomere length
generally declines, but there is wide variability
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Telomeres are non-gene DNA at the ends of DNA strands.
Telomeres are more sensitive to DNA damage, and may act as a sensor for overall DNA damage levels in a cell.
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Does telomere length indicate longevity?
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THE LANCET • Vol 361 • pg 393
Telomere length and mortality in people over 60 years old
upper 50% of telomere length
lower 50% of telomere length
proportion surviving %
years after initial assessment
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Telomere length may indicate biological age.
Early stress may cause premature telomere degradation.
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Fig. 3 TRENDS in Ecology and Evolution Vol 21 pg 47
Balance between Longevity and Health
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Exam 1 score (100pts) = take-home + in-class
Proposal = 5 points of 20 point ExperimentApproved- start collecting dataApproved with changes- after changes, start collecting dataNot approved- Need to resubmit new proposal. Do not collect data until new proposal is approved.Original proposal will be turned in with report (Do not lose it.)